Canonical Allele Identifier: CA399926647

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845693G>A , CM000679.2:g.56845693G>A GRCh38
NC_000017.10:g.54923054G>A , CM000679.1:g.54923054G>A GRCh37
NC_000017.9:g.52278053G>A NCBI36
NG_033888.1:g.16595G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.628G>A (DGKE) MANE Select ENSP00000284061.3:p.Ala210Thr
ENST00000648772.1:c.*314-1903C>T (TRIM25) ENSP00000498158.1:n.*314-1903C>T
ENST00000284061.7:c.628G>A (DGKE) ENSP00000284061.3:p.Ala210Thr
ENST00000571084.1:n.164G>A (DGKE)
ENST00000572944.1:c.458G>A (DGKE)
ENST00000576869.5:n.776G>A (DGKE)
NM_003647.2:c.628G>A (DGKE) NP_003638.1:p.Ala210Thr
XM_011525394.1:c.682G>A (DGKE) XP_011523696.1:p.Ala228Thr
XM_011525395.1:c.682G>A (DGKE) XP_011523697.1:p.Ala228Thr
XM_011525396.1:c.682G>A (DGKE) XP_011523698.1:p.Ala228Thr
XM_011525397.1:c.682G>A (DGKE) XP_011523699.1:p.Ala228Thr
XM_011525398.1:c.172G>A (DGKE) XP_011523700.1:p.Ala58Thr
XR_934581.1:n.781G>A (DGKE)
XM_011525394.3:c.682G>A (DGKE) XP_011523696.1:p.Ala228Thr
XM_011525395.2:c.682G>A (DGKE) XP_011523697.1:p.Ala228Thr
XM_011525396.2:c.682G>A (DGKE) XP_011523698.1:p.Ala228Thr
XM_017025243.2:c.628G>A (DGKE) XP_016880732.1:p.Ala210Thr
XM_017025244.2:c.682G>A (DGKE) XP_016880733.1:p.Ala228Thr
XR_001752670.2:n.814G>A (DGKE)
XR_001752671.1:n.793G>A (DGKE)
XR_001752672.1:n.794G>A (DGKE)
XR_002958079.1:n.792G>A (DGKE)
NM_003647.3:c.628G>A (DGKE) MANE Select NP_003638.1:p.Ala210Thr